Allele Registry

Canonical Allele Identifier: PA2825619455

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001069890

ClinVar Variation:

863031

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Pro514Gln	CA368975004 NM_001127500.3:c.1541C>A